Structure Information
Structure

Compound Identification

SMILES

CC(=O)CCCCC(=O)NCCCCNC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)[C@H]2OC(C)(C)O[C@@H]12

InChIKey

InChIKey=ATVAQHJRFXPIQN-UGTJMOTHSA-J

Formula

C24H35N6O15P3

Mass

740.494

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine ribonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Purine ribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside triphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - 6-alkylaminopurine - 6-aminopurine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Ketal - Secondary aliphatic/aromatic amine - Fatty amide - Monosaccharide - N-acyl-amine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Fatty acyl - Pyrimidine - Imidolactam - Alkyl phosphate - Heteroaromatic compound - Oxolane - Azole - Meta-dioxolane - Imidazole - Carboxamide group - Secondary carboxylic acid amide - Ketone - Carboxylic acid derivative - Organoheterocyclic compound - Acetal - Azacycle - Oxacycle - Hydrocarbon derivative - Organooxygen compound - Organopnictogen compound - Organic oxide - Organic nitrogen compound - Aldehyde - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside triphosphates. These are purine ribobucleotides with a triphosphate group linked to the ribose moiety.

External Descriptors

Not available

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